Trials / Recruiting
RecruitingNCT07006142
Effect of Prolonged Fasting Time on Gastric Residual Volume in Patients Taking GLP1 Receptor Agonists
- Status
- Recruiting
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 150 (estimated)
- Sponsor
- Mayo Clinic · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The aim of this study is to determine whether a modified fasting protocol can reduce the potential risk of aspiration for patients currently prescribed GLP1-RAs.
Detailed description
The overall objective of this project is to identify a reasonable means by which patients on GLP1-RAs can be safely cared for in the perioperative period that can be agreed upon by all groups involved in perioperative patient care. This will be assessed in patients undergoing upper endoscopy specifically since assessment of gastric contents would be minimally invasive for this patient population receiving anesthetic care.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| OTHER | Modified Fasting Guidelines | Patients will follow a full-liquid diet 48 hours prior to their procedure, clear liquid diet 24 hours prior to their procedure, and nothing by mouth (NPO) after midnight on the day of their procedure |
Timeline
- Start date
- 2025-08-01
- Primary completion
- 2026-04-30
- Completion
- 2026-04-30
- First posted
- 2025-06-05
- Last updated
- 2026-02-03
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT07006142. Inclusion in this directory is not an endorsement.